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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433674Generated: November 1, 2026

Water → 4-(Benzyloxy)-2-methylaniline

https://huagongshe.com/reaction/1433674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
Reactant4-Amino-m-cresolHCID 17819—
ReactantSodium hydrideHCID 24758—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl acetate hexaneHCID 21226206—
SolventEther tetrahydrofuranHCID 21868444—
Product4-(Benzyloxy)-2-methylanilineHCID 1677305375.7%

Reaction Steps

After dissolving 4-amino-3-cresol (10 g, 81.20 mmol) in dimethylsulfoxide (80 ml), sodium hydride (3.25 g, 81.20 mmol, 60% in oil) was added and the mixture was stirred for 15 minutes at room temperature under a nitrogen atmosphere. Benzyl bromide (4.83 ml, 40.60 mmol) was added, and the mixture was stirred overnight at room temperature under a nitrogen atmosphere. Water was added to the reaction solution, extraction was performed with diethyl ether/tetrahydrofuran, the extract was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was adsorbed onto silica gel, purified by silica gel column chromatography (hexane-ethyl acetate-ethanol) and then by NH silica gel column chromatography (hexane-ethyl acetate) to obtain the title compound (6.55 g, 30.72 mmol, 75.64%) as a violet oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612092B2
Source datasetuspto-grants-2009_11
ORD IDord-6a5c199c0a7d479cba5181e6c00d2177
Source noteuspto-grants-2009_11